| Literature DB >> 31092921 |
Jordi Guiu1, Edouard Hannezo2,3, Shiro Yui1,4, Samuel Demharter1, Svetlana Ulyanchenko1, Martti Maimets1, Anne Jørgensen5, Signe Perlman6, Lene Lundvall6, Linn Salto Mamsen7, Agnete Larsen8, Rasmus H Olesen8, Claus Yding Andersen7, Lea Langhoff Thuesen9, Kristine Juul Hare9, Tune H Pers10, Konstantin Khodosevich1, Benjamin D Simons2,11,12, Kim B Jensen13,14.
Abstract
Adult intestinal stem cells are located at the bottom of crypts of Lieberkühn, where they express markers such as LGR51,2 and fuel the constant replenishment of the intestinal epithelium1. Although fetal LGR5-expressing cells can give rise to adult intestinal stem cells3,4, it remains unclear whether this population in the patterned epithelium represents unique intestinal stem-cell precursors. Here we show, using unbiased quantitative lineage-tracing approaches, biophysical modelling and intestinal transplantation, that all cells of the mouse intestinal epithelium-irrespective of their location and pattern of LGR5 expression in the fetal gut tube-contribute actively to the adult intestinal stem cell pool. Using 3D imaging, we find that during fetal development the villus undergoes gross remodelling and fission. This brings epithelial cells from the non-proliferative villus into the proliferative intervillus region, which enables them to contribute to the adult stem-cell niche. Our results demonstrate that large-scale remodelling of the intestinal wall and cell-fate specification are closely linked. Moreover, these findings provide a direct link between the observed plasticity and cellular reprogramming of differentiating cells in adult tissues following damage5-9, revealing that stem-cell identity is an induced rather than a hardwired property.Entities:
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Year: 2019 PMID: 31092921 PMCID: PMC6986928 DOI: 10.1038/s41586-019-1212-5
Source DB: PubMed Journal: Nature ISSN: 0028-0836 Impact factor: 49.962